تفاعل #5355

ord-bdf94d64f6764381bbbb7b18839e7b85

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONare added
  2. 2
    استخلاصextracted three times with ethyl acetate
  3. 3
    غسيلThe combined organic layers are washed with brine
  4. 4
    تجفيفdried over Na2SO4
  5. 5
    تركيزconcentrated in vacuo
  6. 6
    أخرىThe residue is purified via flash chromatography on a 40 mm×150 mm silica gel column
  7. 7
    غسيلeluting with 5% methanol/ethyl acetate

الإجراء التجريبي

To a stirring solution of 189 mg (1.89 mmol) of tetronic acid in 15 mL of dimethylformamide is added 290 μL (2.08 mmol) of triethylamine and 8 mg (66 μmol) of 4-dimethylaminopyridine at 0° C. Next, 427 mg (2.22 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 690 mg (2.20 mmol) of 10-(4-chlorophenyl)dec-9-enoic acid as a mixture of E and Z isomers are added and the reaction mixture is stirred overnight at room temperature. The reaction is acidified with 1.0N HCl and extracted three times with ethyl acetate. The combined organic layers are washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue is purified via flash chromatography on a 40 mm×150 mm silica gel column eluting with 5% methanol/ethyl acetate to give 400 mg (58%) of pure 4-hydroxy-3-[10-(4-chlorophenyl)-1-oxodec-9-enyl] -2(5H)-furanone as a mixture of E and Z isomers.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05242945uspto-grants-1993_09